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2-Cyclopenten-1-one, 2,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62156-62-1

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62156-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62156-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,5 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62156-62:
(7*6)+(6*2)+(5*1)+(4*5)+(3*6)+(2*6)+(1*2)=111
111 % 10 = 1
So 62156-62-1 is a valid CAS Registry Number.

62156-62-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-diphenylcyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Cyclopenten-1-one,2,5-diphenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62156-62-1 SDS

62156-62-1Downstream Products

62156-62-1Relevant academic research and scientific papers

Iodine-Catalyzed Iso-Nazarov Cyclization of Conjugated Dienals for the Synthesis of 2-Cyclopentenones

Marsili, Lucía A.,Pergomet, Jorgelina L.,Gandon, Vincent,Riveira, Martín J.

supporting information, p. 7298 - 7303 (2018/11/25)

Molecular iodine was identified as an efficient catalyst for the cycloisomerization of conjugated dienals to substituted 2-cyclopentenones. DFT calculations suggested an unexpected concerted character for this cyclization.

Reaction of Alkynes with Cyclopropylcarbene-Chromium Complexes: A Versatile Cycloaddition Reaction for the Construction of Cyclopentenones

Tumer, Seniz U.,Herndon, James W.,McMullen, Leonard A.

, p. 8394 - 8404 (2007/10/02)

The scope and limitations of the reaction between cyclopropylcarbene-chromium complexes and alkynes have been examined.A variety of cyclopropylcarbene complexes and alkynes have been employed in these studies.The reaction appears to be general for most simple alkynes, producing cyclopentenones.A mechanism has been proposed involving metallacyclobutene formation, electrocyclic ring opening, electrocyclic ring closure, CO insertion, alkene insertion, metallacyclopentene fragmentation and cyclopentadienone reduction.The presence of these intermediates has been inferred from the structure of products obtained when the reaction was conducted in acetonitrile instead of dioxane.A trapping experiment employing 1,6-heptadiyne supports the intermediacy of vinylcarbene or vinylketene complexes.

Carbonylation of Enynes under Hydroformylation Conditions Catalyzed by Rhodium Carbonyl. A New Method for Synthesis of Cyclic Enones

Doyama, Kazuo,Joh, Takashi,Shiohara, Tomoo,Takahashi, Shigetoshi

, p. 4353 - 4360 (2007/10/02)

The reactivities of 1-buten-3-yne derivatives toward hydroformylation were studied using a rhodium catalyst.Unexpectedly, cyclopentenone derivatives were obtained in moderate yields together with formyl-substituted dienes and unsaturated lactones.This rea

HYDROFORMYLATION AND HYDROCARBONYLATION OF ENYMES BY RHODIUM CARBONYL CLUSTER: A NEW ROUTE TO CYCLIC ENONES

Doyama, Kazuo,Joh, Takashi,Takahashi, Shigetoshi

, p. 4497 - 4500 (2007/10/02)

The reaction of but-1-en-3-yne derivates with carbon monoxide and hydrogen in the presence of Rh4(CO)12 catalyst gave formyl-dienes, cyclopentenones and unsaturated lactones, which shows the CC is much more reactive than the C=C moiety and may provide

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